| Approved symbol | PRPH2 |
|---|---|
| Approved name | peripherin 2 |
| HGCN ID | HGNC:9942 |
| Previous symbols | RP7, RDS |
| Inheritance | |
| OMIM | 179605 |
| Chromosome | 6p21.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB PRPH2 Analysis |
